Hallam Bradley J, Jacova Claudia, Hsiung Ging-Yuek R, Wittenberg Dana, Sengdy Pheth, Bouchard-Kerr Phoenix, Slack Penny, Rademakers Rosa, Baker Matthew, Chow Tiffany W, Levine Brian, Feldman Howard H, Mackenzie Ian R
1Department of Medicine,Division of Neurology,University of British Columbia,Vancouver,British Columbia,Canada.
2Department of Neuroscience,Mayo Clinic,Jacksonville,Florida.
J Int Neuropsychol Soc. 2014 Aug;20(7):694-703. doi: 10.1017/S1355617714000551. Epub 2014 Jul 4.
Mutations in the progranulin gene (GRN) are a common cause of familial frontotemporal dementia. We used a comprehensive neuropsychological battery to investigate whether early cognitive changes could be detected in GRN mutation carriers before dementia onset. Twenty-four at-risk members from six families with known GRN mutations underwent detailed neuropsychological testing. Group differences were investigated by domains of attention, language, visuospatial function, verbal memory, non-verbal memory, working memory and executive function. There was a trend for mutation carriers (n=8) to perform more poorly than non-carriers (n=16) across neuropsychological domains, with significant between group differences for visuospatial function (p<.04; d=0.92) and working memory function (p<.02; d=1.10). Measurable cognitive differences exist before the development of frontotemporal dementia in subjects with GRN mutations. The neuropsychological profile of mutation carriers suggests early asymmetric, right hemisphere brain dysfunction that is consistent with recent functional imaging data from our research group and the broader literature.
原纤维蛋白基因(GRN)突变是家族性额颞叶痴呆的常见病因。我们使用一套全面的神经心理学测试组合,来研究在痴呆症发作前,能否在GRN突变携带者中检测到早期认知变化。来自六个已知GRN突变家族的24名高危成员接受了详细的神经心理学测试。通过注意力、语言、视觉空间功能、言语记忆、非言语记忆、工作记忆和执行功能等领域来研究组间差异。在各个神经心理学领域,突变携带者(n = 8)的表现往往比非携带者(n = 16)更差,其中视觉空间功能(p <.04;d = 0.92)和工作记忆功能(p <.02;d = 1.10)在组间存在显著差异。在患有GRN突变的受试者中,在额颞叶痴呆发展之前就存在可测量的认知差异。突变携带者的神经心理学特征表明存在早期不对称的右半球脑功能障碍,这与我们研究小组最近获得的功能成像数据以及更广泛的文献一致。